Pages that link to "Q59080097"
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The following pages link to Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells (Q59080097):
Displayed 30 items.
- Semidominance of rad18-2 for several phenotypic characters in Saccharomyces cerevisiae (Q33949960) (← links)
- Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect (Q35201815) (← links)
- The identification of fanconi anemia genotypes by clastogenic stress (Q35202474) (← links)
- Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods (Q35202930) (← links)
- Sister chromatid exchange analysis (Q35203856) (← links)
- Genetic susceptibility to iatrogenic malignancy (Q36249238) (← links)
- Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment (Q36630840) (← links)
- Abnormal response to DNA crosslinking agents of Fanconi anemia fibroblasts can be corrected by transfection with normal human DNA. (Q37399881) (← links)
- 1,3-Butadiene: II. Genotoxicity profile (Q37792078) (← links)
- Genetic instability in the human population: A working hypothesis1,2 (Q40135137) (← links)
- Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospects. (Q40245324) (← links)
- Genetic predisposition to cancer in man: in vitro studies. (Q40249069) (← links)
- Dna repair: pathways and defects (Q40296821) (← links)
- DNA repair dependent NAD+ metabolism is impaired in cells from patients with Fanconi's anemia (Q41452492) (← links)
- Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane (Q44411742) (← links)
- Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay. (Q54331645) (← links)
- Spontaneous 6-thioguanine-resistant lymphocytes in Fanconi anemia patients and their heterozygous parents. (Q54457206) (← links)
- DNA semi-conservative synthesis in normal and Fanconi anemia fibroblasts following treatment with 8-methoxypsoralen and near ultraviolet light or with X-rays. (Q54696998) (← links)
- Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype. (Q54856855) (← links)
- Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes (Q58194251) (← links)
- Mutagenic effects of isonicotinic acid hydracide in Fanconi's anemia (Q66993295) (← links)
- Intracellular distribution of DNA topoisomerase I in fibroblasts from patients with Fanconi's anaemia (Q67256328) (← links)
- Proliferative kinetics and mitomycin C-induced chromosome damage in Fanconi's anemia lymphocytes (Q70428301) (← links)
- The cell cycle of lymphocytes in Fanconi anemia (Q70578804) (← links)
- Reduced uptake and incorporation of 3H-thymidine in Fanconi anemia fibroblasts (Q70827964) (← links)
- Prenatal diagnosis of Fanconi anemia (Q70999378) (← links)
- Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts (Q71438274) (← links)
- Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system (Q71826957) (← links)
- Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia (Q71843008) (← links)
- Fanconi's anemia: anomaly of enzyme passage through the nuclear membrane? Anomalous intracellular distribution of topoisomerase activity in placental extracts in a case of Fanconi's anemia (Q72908823) (← links)